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QA Specialist CSV

Fidel Consulting KK

Chiyoda City, Tokyo, Japan Full-time July 01, 2026
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Opportunity Description

 Appealing Points:



  • Lead Quality & Compliance in Global Pharma IT – Ensure GxP compliance, computer system validation, and data integrity across complex global IT systems and regulated processes.

  • Drive Regulatory Excellence – Lead validation oversight, audit readiness, and quality governance while ensuring compliance with 21 CFR Part 11 and global pharmaceutical standards.

  • Influence Enterprise-Wide Quality Initiatives – Partner with cross-functional global teams to improve validation processes, q...
Full-time Computer Occupations

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